A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5845381



Internal ID22620316
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:62888708..62935825hg38UCSC Ensembl
chr6:63598613..63645730hg19UCSC Ensembl
Cytoband6q12
Allele length
AssemblyAllele length
hg3847118
hg1947118
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17507253
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5845381
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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